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“FERNO” BACKBOARD STRETCHER (Non-Sterile) - Taiwan Registration bfbb6358d304d56351445538d0dc9f37

Access comprehensive regulatory information for “FERNO” BACKBOARD STRETCHER (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bfbb6358d304d56351445538d0dc9f37 and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is EZ-CARE INSTRUMENTS. CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FERNO-WASHINGTON, INC., and 3 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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bfbb6358d304d56351445538d0dc9f37
Registration Details
Taiwan FDA Registration: bfbb6358d304d56351445538d0dc9f37
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Device Details

“FERNO” BACKBOARD STRETCHER (Non-Sterile)
TW: “婓諾” 長背板擔架 (未滅菌)
Risk Class 1
MD

Registration Details

bfbb6358d304d56351445538d0dc9f37

Ministry of Health Medical Device Import Registration No. 015780

DHA08401578008

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Portable Stretcher (J.6900)".

J General hospital and personal use equipment

J6900 portable stretcher

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

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